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SARAH Exercise Program in Patients With Rheumatoid Arthritis

Investigating the Effects of SARAH Exercise Program on Proprioception and Hand Functions in Patients With Rheumatoid Arthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05727488
Enrollment
49
Registered
2023-02-14
Start date
2023-11-16
Completion date
2024-06-26
Last updated
2024-07-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rheumatoid Arthritis

Keywords

Hand, Proprioception, Exercise

Brief summary

The aim of this study is to investigate the effectiveness of the SARAH home exercise program to be applied for 12 weeks on wrist proprioception and hand functions in adult patients with rheumatoid arthritis.

Detailed description

Finger/hand/wrist joints can be affected in the early period in patients with RA, and as the disease progresses, it can significantly limit the patient's functionality. Damage to articular and periarticular structures seen in inflammatory arthritis may affect the sense of proprioception by destroying mechanoreceptors located in these areas. Hand functions may worsen as a result of the worsening of the sense of proprioception, which can be defined as being aware of body parts. SARAH (Strengthening and Stretching for Rheumatoid Arthritis of the Hand) home exercise program, which is a widely preferred approach in the case of hand involvement in patients with rheumatoid arthritis (RA), includes exercises to increase hand-wrist strength and mobility. Although the effectiveness of this program on pain, muscle strength, and range of motion has been demonstrated in large patient groups, its effect on proprioception and hand functions, which may be caused by inflammatory arthritis, has not been studied. Therefore, this study aims to investigate the effectiveness of the SARAH home exercise program on wrist proprioception and hand functions in adult patients with rheumatoid arthritis.

Interventions

OTHERExercise

Participants will be asked to practice home exercises every day of the week for 12 weeks. The SARAH exercise program consists of 7 mobility and 4 strengthening exercises. Progress will be made by increasing the repetitions and duration of the exercises every week.

Sponsors

Izmir Katip Celebi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. RA diagnosis according to 2010 ACR/EULAR RA criteria 2. Being between the ages of 18-65 3. Being able to follow Turkish instructions 4. Volunteering to participate in the study

Exclusion criteria

1. Being in an acute disease exacerbation period 2. Ongoing physiotherapy/occupational/exercise treatment regarding hands within the last 6 months 3. History of steroid injection, surgery, or trauma to the upper extremity in the last 6 months

Design outcomes

Primary

MeasureTime frameDescription
Change in Self-reported Hand FunctionsAt baseline and twelve weeks laterDuruoz Hand Index and The Measures of Activity Performance of the Hand Questionnaire will be used for subjective assessment of hand functions. Higher scores in both questionnaires reflect poorer hand functions.
Change in Wrist Joint Position SenseAt baseline and twelve weeks laterWrist joint position sense will be evaluated with joint position sense goniometry. Joint position sense is measured by the ability to actively repeat a predetermined target angle. During the measurement, the wrist of the participant will passively be brought to the target angle and be kept in this position for three seconds. The participant will be asked to keep this position in his/her memory, then the wrist will passively be brought to the starting position. Then, the participant will be requested to bring her/his hand actively to these predetermined position. Wrist movements will be determined as three repetitive measurements for flexion, extension, radial deviation, and ulnar deviation directions.
Change in Hand PerformanceAt baseline and twelve weeks laterHand performance will be evaluated Nine-Hole Peg Test.
Change in Grip StrengthAt baseline and twelve weeks laterHand grip strength will be evaluated with a hand-dynamometer.
Change in Pinch StrengthAt baseline and twelve weeks laterPinch strength will be evaluated by using a pinchmeter.

Secondary

MeasureTime frameDescription
Change in Morning StiffnessAt baseline and twelve weeks laterMorning stiffness related to the hand/wrist of the patients will be questioned by using Numeric Rating Scale (0-10) in terms of duration and severity. Higher scores indicate worse morning stiffness.
Change in Disease ActivityAt baseline and twelve weeks laterDisease Activity 28 C-Reactive Protein (DAS28-CRP) will be used to evaluate disease activity.
Change in General FunctioningAt baseline and twelve weeks laterHealth Assessments Questionnaire-Disability Index, which is a self-report tool and has 20 items, will be used to evaluate the general functioning. All items are scored between 0 and 3. All scores are summed and divided by 20 to obtain a total score (0-3). Higher scores indicate a worse functional status.
Change in PainAt baseline and twelve weeks laterNumeric rating scale (NRS) will be used for pain assessment. NRS is scored between 0-10 and, higher scores indicate higher level of pain.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026